HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373663Generated: October 25, 2026
Adenosine Monophosphate → HCID 178508926, compound
https://huagongshe.com/reaction/373663
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Adenosine Monophosphate | HCID 6083 | — |
| Reactant | 2-Aminooxetanocin A | HCID 451559 | — |
| Solvent | Phosphate | HCID 1061 | — |
| Product | HCID 178508926 | HCID 178508926 | — |
Reaction Steps
After 2.0 g of 2-amino-OXT-A was dissolved in 300 ml of 1/10M phosphate buffer (pH 6.5), 8.0 g of 5'-adenylic acid deaminase (manufactured by Amano Pharmaceutical Co., Ltd., DEAMIZYME®) was added to the solution followed by stirring at 37° C. for 70 hours. After insoluble matters of the reaction solution were removed by filtration, the filtrate was passed through a column packed with 50 ml of activated charcoal powders (manufactured by Wako Pure Chemical Industry K.K., for chromatography). After washing with water, elution was performed with 50% aqueous methanol. By concentrating the desired fraction to dryness, crude OXT-G was obtained. The crude powders were dissolved in 50 ml of water and the OXT-G in the solution was adsorbed onto MCI® GEL CHP 20 (300 ml) followed by elution with water. The desired fraction was concentrated and evaporated to dryness under reduced pressure to give 1.5 g of OXT-G as colorless crystals (yield, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05164500 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-152f04f6ff8c402b83461295500c4937 |
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| Source note | uspto-grants-1992_11 |
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